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Medical Forum / Diseases and Disorders / Alzheimer's / August 2004

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Brain ferrous toxic iron

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doe - 18 Aug 2004 17:37 GMT
<<snip>>
presence of hemosiderin together with ferritin in the pathological brains
<<snip>>

J Struct Biol. 2004 Aug;147(2):166-78.  Related Articles, Links  

 
Electron nanodiffraction and high-resolution electron microscopy studies of the
structure and composition of physiological and pathological ferritin.

Quintana C, Cowley JM, Marhic C.

Instituto de Microelectronica de Madrid. C.S.I.C., 8 Isaac Newton, PTM, 28760
Tres Cantos Madrid, Spain.

Structures of core nanocrystals of physiological (horse spleen, human liver,
and brain) and pathological human brain of patients with progressive
supranuclear palsy (PSP) and Alzheimer's disease (AD) ferritin molecules were
determined using electron nanodiffraction and high-resolution transmission
electron microscopy. The poly-phasic structure of the ferritin cores is
confirmed. There are significant differences in the mineral composition between
the physiological and pathological ferritins. The physiological ferritin cores
mainly consist of single nanocrystals containing hexagonal ferrihydrite (Fh)
and hematite (Hm) and some cubic magnetite/maghemite phase. In the pathological
cores, Fh is present but only as a minor phase and Hm is absent. The major
phases are a face-centered-cubic (fcc) structure with [Formula: see text] nm
and a high degree of disorder, related to wustite, and a cubic magnetite-like
structure. These two cubic phases are also present in human aged normal brain.
Evidence for the presence of hemosiderin together with ferritin in the
pathological brains is deduced from the similarities of the diffraction
patterns with those from patients with primary hemochromatosis, and differences
in the shapes and protein composition of the protein shell. These findings
suggest a disfunction of the ferritin associated with PSP and AD, associated
with an increase in the concentration of brain ferrous toxic iron.

PMID: 15193645 [PubMed - in process]

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Nightwing - 22 Aug 2004 04:02 GMT
doe you are an idiot
john malins - 26 Aug 2004 21:46 GMT
> doe you are an idiot
>
> Yes I agree with you,the mans a fool! he pedals his old iron   on many
newsgroups ,according to him all of our diseases are caused by the presence
of iron,everything from in growing  toe nails to Alzheimer's.makes you
wonder how the human species' ever evolved with  this" poisonous "iron
everywhere in plants and animals.And it is these sort of crackpot ideas that
cause anxiety to many people who are in a vulnerable  and emotional
situation looking after their family ,but of course he says that Jesus was a
vegetarian! what nonsense,Christ frequently referred to sheep ,Oxon,
fishes,he even told the fishermen where to cast there nets.        I know
I'm getting away from the point ,but don't get drawn into believing his
rusty theories         john.m
doe - 28 Aug 2004 13:53 GMT
>Subject: Re: Brain ferrous toxic iron

Ann N Y Acad Sci. 2004 Mar;1012:179-182.  Related Articles, Links  

 
Oxidative Stress and Redox-Active Iron in Alzheimer's Disease.

Honda K, Casadesus G, Petersen RB, Perry G, Smith MA.

Institute of Pathology, Case Western Reserve University, Cleveland, Ohio, USA.

Many lines of evidence indicate that oxidative stress is one of the earliest
events in the genesis of Alzheimer's disease (AD). Iron is a transition metal
capable of generating hydroxyl radicals, the most potent reactive oxygen
species. Consequently, a disruption in the metabolism of iron has been
postulated to have a role in the pathogenesis of AD. Indeed, both senile
plaques and neurofibrillary tangles, the major pathological landmarks of AD, as
well as neurons in the earliest stages of the disease, show elevated iron
deposition. However, it is clear that the iron bound to lesion-associated
proteins such as amyloid-beta and tau plays only a minor, late role in the
disease, with the RNA-associated iron found in the neuronal cytoplasm occurring
early and being of paramount importance. In this regard, it is probably not
surprising that there is significant oxidation of cytoplasmic RNA among the
populations of neurons vulnerable to AD. In this review, we consider the role
of iron-induced oxidative stress as a key event in AD pathophysiology.

PMID: 15105265 [PubMed - as supplied by publisher]

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Who loves ya.
Tom
doe - 28 Aug 2004 15:27 GMT
>Subject: Brain ferrous toxic iron

Free Radic Biol Med. 2001 Feb 15;30(4):447-50.  Related Articles, Links  

 
Redox-active iron mediates amyloid-beta toxicity.

Rottkamp CA, Raina AK, Zhu X, Gaier E, Bush AI, Atwood CS, Chevion M, Perry G,
Smith MA.

Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106,
USA.

While amyloid-beta toxicity is mediated by oxidative stress and can be
attenuated by antioxidants, the actual biochemical mechanism underlying
neurotoxicity remains to be established. However, since aggregated amyloid-beta
can interact with transition metals, such as iron, both in vitro and in vivo,
we suspected that bound iron might be the mediator of toxicity such that holo-
and apo-amyloid would have differential effects on cellular viability. Here we
demonstrate that when amyloid-beta is pretreated with the iron chelator
deferoxamine, neuronal toxicity is significantly attenuated while conversely,
incubation of holo-amyloid-beta with excess free iron restores toxicity to
original levels. These data, taken together with the known sequelae of
amyloid-beta, suggest that the toxicity of amyloid-beta is mediated, at least
in part, via redox-active iron that precipitates lipid peroxidation and
cellular oxidative stress.

PMID: 11182300 [PubMed - indexed for MEDLINE]

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Who loves ya.
Tom
Signature

Jesus Was A Vegetarian! http://jesuswasavegetarian.7h.com
Man Is A Herbivore! http://pages.ivillage.com/ironjustice/manisaherbivore
DEAD PEOPLE WALKING http://pages.ivillage.com/ironjustice/deadpeoplewalking

 
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